NDC 10742-8162

Rohto Dry-Aid

Povidone, Propylene Glycol

Rohto Dry-Aid is a Ophthalmic Liquid in the Human Otc Drug category. It is labeled and distributed by The Mentholatum Company. The primary component is Povidone, Unspecified; Propylene Glycol.

• Product ID: 10742-8162_4b62eec2-64cc-4f87-adee-13d266baa388
• NDC: 10742-8162
• Product Type: Human Otc Drug
• Proprietary Name: Rohto Dry-Aid
• Generic Name: Povidone, Propylene Glycol
• Dosage Form: Liquid
• Route of Administration: OPHTHALMIC
• Marketing Start Date: 2017-01-01
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part349
• Labeler Name: The Mentholatum Company
• Substance Name: POVIDONE, UNSPECIFIED; PROPYLENE GLYCOL
• Active Ingredient Strength: 7 mg/mL; mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 10742-8162-1

1 BOTTLE, DROPPER in 1 CARTON (10742-8162-1) > 10 mL in 1 BOTTLE, DROPPER

• Marketing Start Date: 2017-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10742-8162-2 [10742816202]

Rohto Dry-Aid LIQUID

• Marketing Category: OTC monograph final
• Application Number: part349
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-01-01

NDC 10742-8162-1 [10742816201]

Rohto Dry-Aid LIQUID

• Marketing Category: OTC monograph final
• Application Number: part349
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-01-01

Drug Details

Active Ingredients

Ingredient	Strength
POVIDONE, UNSPECIFIED	6.8 mg/mL

OpenFDA Data

• SPL SET ID: 8ea5c6c9-48f4-406a-a2cb-9280c546d87d
• Manufacturer:
  • The Mentholatum Company
• UNII:
  • FZ989GH94E
  • 6DC9Q167V3
• RxNorm Concept Unique ID - RxCUI:
  • 1863574

NDC Crossover Matching brand name "Rohto Dry-Aid" or generic name "Povidone, Propylene Glycol"

NDC	Brand Name	Generic Name
10742-8162	Rohto Dry-Aid	povidone, propylene glycol
49873-503	Dorama Dry Aid Eye Drops	povidone, propylene glycol
10742-8161	Rohto	povidone, propylene glycol